Planta

, Volume 229, Issue 1, pp 87–98

Expression of callose synthase genes and its connection with Npr1 signaling pathway during pathogen infection

  • Xiaoyun Dong
  • Zonglie Hong
  • Jayanta Chatterjee
  • Sunghan Kim
  • Desh Pal S. Verma
Original Article

DOI: 10.1007/s00425-008-0812-3

Cite this article as:
Dong, X., Hong, Z., Chatterjee, J. et al. Planta (2008) 229: 87. doi:10.1007/s00425-008-0812-3

Abstract

Callose synthesis occurs at specific stages of plant cell wall development in all cell types, and in response to pathogen attack, wounding and physiological stresses. We determined the expression pattern of “upstream regulatory sequence” of 12 Arabidopsis callose synthase genes (CalS112) genes and demonstrated that different callose synthases are expressed specifically in different tissues during plant development. That multiple CalS genes are expressed in the same cell type suggests the possibility that CalS complex may be constituted by heteromeric subunits. Five CalS genes were induced by pathogen (Hyaloperonospora arabidopsis, previously known as Peronospora parasitica, the causal agent of downy mildew) or salicylic acid (SA), while the other seven CalS genes were not affected by these treatments. Among the genes that are induced, CalS1 and CalS12 showed the highest responses. In Arabidopsis npr1 mutant, impaired in response of pathogenesis related (PR) genes to SA, the induction of CalS1 and CalS12 genes by the SA or pathogen treatments was significantly reduced. The patterns of expression of the other three CalS genes were not changed significantly in the npr1 mutant. These results suggest that the high induction observed of CalS1 and CalS12 is Npr1 dependent while the weak induction of five CalS genes is Npr1 independent. In a T-DNA knockout mutant of CalS12, callose encasement around the haustoria on the infected leaves was reduced and the mutant was found to be more resistant to downy mildew as compared to the wild type plants.

Keywords

CalloseDowny mildewGene expressionTissue specific promoterSalicylic acidPlant pathogenCell wall

Abbreviations

as-1

Activating sequence 1

BTH

Benzothiadiazole

CalS

Callose synthase

Gsl

Glucan synthase-like

GUS

β-glucuronidase

JA

Jasmonic acid

MeJA

Methyl jasmonic acid

NahG

Naphthalene (salicylate) hydroxylase G

Npr1

Nonexpresser of PR genes

pmr4

Powdery mildew resistant 4

SA

Salicylic acid

SAR

Systemic acquired resistance

TGA

cis-acting element TGACG

TGA-Bzip

The basic leucine zipper transcription factors that recognize cis-acting element TGACG

W-box

cis-acting element (TTGAC) that is recognized by WRKY proteins

WRKY proteins

DNA-binding proteins containing a highly conserved WRKY sequence

Supplementary material

425_2008_812_MOESM1_ESM.doc (28 kb)
Supplemental Tables I and II (DOC 28 kb)

Copyright information

© Springer-Verlag 2008

Authors and Affiliations

  • Xiaoyun Dong
    • 1
    • 3
  • Zonglie Hong
    • 2
    • 4
  • Jayanta Chatterjee
    • 2
  • Sunghan Kim
    • 2
  • Desh Pal S. Verma
    • 1
  1. 1.Plant Biotechnology Center, Department of Plant Pathology and Department of Molecular GeneticsThe Ohio State UniversityColumbusUSA
  2. 2.Plant Biotechnology Center and Department of Molecular GeneticsThe Ohio State UniversityColumbusUSA
  3. 3.The Children’s Hospital of PhiladelphiaPhiladelphiaUSA
  4. 4.Department of Microbiology, Molecular Biology and BiochemistryUniversity of IdahoMoscowUSA